Canonical Allele Identifier: CA4070989

Gene: SERAC1

Linked Data

• dbSNP Id: rs538774632
• ExAC: 6:158535756 TTTC / T
• gnomAD v2: 6-158535756-TTTC-T
• gnomAD v3: 6-158114724-TTTC-T
• gnomAD v4: 6-158114724-TTTC-T
• MyVariant Identifiers: chr6:g.158535757_158535759del (hg19) ; chr6:g.158114725_158114727del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114732_158114734del , CM000668.2:g.158114732_158114734del	GRCh38
NC_000006.11:g.158535764_158535766del , CM000668.1:g.158535764_158535766del	GRCh37
NC_000006.10:g.158455752_158455754del	NCBI36
NG_032889.1:g.58554_58556del

Transcript Alleles

HGVS	Amino-acid change
ENST00000607071.6:c.*1404+62_*1404+64del	ENSP00000475855.1:n.*1404+62_*1404+64del
ENST00000642244.1:c.1594+62_1594+64del	ENSP00000493554.1:n.1594+62_1594+64del
ENST00000642903.1:c.1746_1748del	ENSP00000493559.1:p.Lys583del
ENST00000644972.1:c.1684+62_1684+64del	ENSP00000496451.1:n.1684+62_1684+64del
ENST00000645077.1:c.*1305+62_*1305+64del	ENSP00000496113.1:n.*1305+62_*1305+64del
ENST00000645172.1:c.*1386+62_*1386+64del	ENSP00000495367.1:n.*1386+62_*1386+64del
ENST00000646190.1:n.3015+62_3015+64del
ENST00000646208.1:c.1420+62_1420+64del	ENSP00000493723.1:n.1420+62_1420+64del
ENST00000646410.1:c.1555+62_1555+64del	ENSP00000494205.1:n.1555+62_1555+64del
ENST00000646562.1:c.*1580_*1582del	ENSP00000496087.1:n.*1580_*1582del
ENST00000647468.2:c.1684+62_1684+64del MANE Select	ENSP00000496731.1:n.1684+62_1684+64del
ENST00000648111.1:c.*1372+62_*1372+64del	ENSP00000497275.1:n.*1372+62_*1372+64del
ENST00000367104.7:c.1684+62_1684+64del	ENSP00000356071.3:n.1684+62_1684+64del
ENST00000435180.5:c.471_473del	ENSP00000391168.1:p.Lys158del
ENST00000606965.5:c.*307_*309del	ENSP00000475808.1:n.*307_*309del
ENST00000607071.5:c.*1618+62_*1618+64del	ENSP00000475855.1:n.*1618+62_*1618+64del
ENST00000607742.5:c.*2962+62_*2962+64del	ENSP00000475523.1:n.*2962+62_*2962+64del
NM_032861.3:c.1684+62_1684+64del	NP_116250.3:n.1684+62_1684+64del
NR_073096.1:n.1679_1681del
XM_006715586.1:c.1474+62_1474+64del	XP_006715649.1:n.1474+62_1474+64del
XM_011536196.1:c.1663+62_1663+64del	XP_011534498.1:n.1663+62_1663+64del
XM_011536197.1:c.1570+62_1570+64del	XP_011534499.1:n.1570+62_1570+64del
XM_011536198.1:c.1474+62_1474+64del	XP_011534500.1:n.1474+62_1474+64del
XM_006715586.3:c.1474+62_1474+64del	XP_006715649.1:n.1474+62_1474+64del
XM_011536196.3:c.1663+62_1663+64del	XP_011534498.1:n.1663+62_1663+64del
XM_011536198.3:c.1474+62_1474+64del	XP_011534500.1:n.1474+62_1474+64del
XM_024446573.1:c.1684+62_1684+64del	XP_024302341.1:n.1684+62_1684+64del
XR_001743697.2:n.1715+62_1715+64del
XR_942606.2:n.1766+62_1766+64del
NM_032861.4:c.1684+62_1684+64del MANE Select	NP_116250.3:n.1684+62_1684+64del
NR_073096.2:n.1661_1663del